Abstract
Lithium and sodium plating are inevitable when using negative electrodes with an electrochemical potential close to one of the charge carriers. Typical testing and modeling assume that plating occurs at 0 V when measured against the charge carrier. While this might be true under thermodynamic equilibrium, this is not true outside of steady state. This has significant implications as, by taking this into account, the testing voltage window of negative electrodes could be extended to allow gathering data for more complete discharges at higher rates. Moreover, from a modeling standpoint, it could also allow us to more accurately predict plating initiation potentials dynamically. This work presents the preliminary results of the investigation of what parameters are influencing the plating potential and how to take them into account in testing and modeling.
| Original language | English |
|---|---|
| Article number | 408 |
| Number of pages | 8 |
| Journal | Batteries |
| Volume | 10 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 21 Nov 2024 |
Bibliographical note
© 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).Funding
This research was funded by ONR grant number N00014-20-1-2270 and the Faraday Institution (EP/S003053/1) via the LiSTAR project (FIRG058).
| Funders | Funder number |
|---|---|
| Office of Naval Research | N00014-20-1-2270 |
| The Faraday Institution | EP/S003053/1, FIRG058 |
Keywords
- degradation modes mechanistic modeling
- lithium plating
- sodium plating
ASJC Scopus subject areas
- Energy Engineering and Power Technology
- Electrochemistry
- Electrical and Electronic Engineering
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